期刊
JOURNAL OF CLINICAL DENSITOMETRY
卷 11, 期 3, 页码 351-359出版社
ELSEVIER SCIENCE INC
DOI: 10.1016/j.jocd.2008.04.001
关键词
bone geometry; denosumab; hip; proximal femur; osteoporosis; RANKL inhibitor
资金
- Amgen Inc
Denosumab is a fully human monoclonal antibody against receptor activator of nuclear factor-kappa B ligand, an essential mediator of osteoclast activity and survival. In post menopausal women with low bone mineral density (BMD). Subcutaneous denosumab decreases bone resorption and increases BMD. This post hoc analysis reports on subjects treated for up to 24 months with denosumab 60 mg 6 monthly (N = 39), placebo (N = 39), or open-label alendronate 70 mg once weekly (N = 38) in a phase 2 study. Hip scans were done by dual-energy X-ray absorptiometry at baseline. 12, and 24 months: these were analyzed with hip structural analysis software to evaluate BMD and cross-sectional geometry parameters at the narrowest segment of the femoral neck, the intertrochanter. and the proximal shaft. Geometric parameters and derived strength indices included bone cross-sectional area, section modulus. and buckling, ratio. At 12 and 24 months denosumab and alendronate improved these parameters compared with placebo. Denosumab effects were greater than alendronate at the intertrochanteric and shaft sites. The magnitude and direction of the changes in structural geometry parameters observed in this study suggest that denosumab treatment may lead to improved bone mechanical properties. Ongoing phase 3 studies will determine whether denosumab reduces fracture risk.
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